NP-MRD: Showing NP-Card for 3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one (NP0166367)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 01:44:32 UTC

Updated at

2022-09-03 01:44:33 UTC

NP-MRD ID

NP0166367

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

Description

Kaempferol 3-apiosyl-(1->2)-alpha-l-arabinofuranoside-7-rhamnoside belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Thus, kaempferol 3-apiosyl-(1->2)-alpha-L-arabinofuranoside-7-rhamnoside is considered to be a flavonoid lipid molecule. 3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one is found in Cinnamomum burmannii and Cinnamomum osmophloeum. Kaempferol 3-apiosyl-(1->2)-alpha-l-arabinofuranoside-7-rhamnoside is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161523002D          

 49 54  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6194    1.3099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8743    2.0945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3894    2.7620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7250    3.5157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993    2.0945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1842    2.7620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9543    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7389    1.0550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3520    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2657    2.4275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0194    2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5715    2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1235    2.7631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2389    1.6650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1527    0.8446    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1590    1.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4945    0.6818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 18 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 26 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 38 42  1  0  0  0  0
 35 42  1  0  0  0  0
 42 43  1  0  0  0  0
  4 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
  2 48  1  0  0  0  0
 48 49  1  0  0  0  0
M  END

     RDKit          3D

 85 90  0  0  0  0  0  0  0  0999 V2000
    6.4877    3.1589    2.4168 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    3.2443    0.9209 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6166    2.2761    0.3333 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0619    0.9832    0.7994 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1941    0.0764    0.2598 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8453   -0.1219    0.4365 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0486    0.7275    1.1830 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6881    0.4720    1.3119 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9249    1.3443    2.0646 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1122   -0.6074    0.7168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2328   -0.9021    0.7999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9581   -0.1390    1.4618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7762   -2.0237    0.1622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1476   -2.2420    0.2719 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0303   -1.5976   -0.6484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6895   -2.5304   -1.4081 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0396   -2.2607   -1.4621 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5615   -2.5050   -2.8712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9216   -2.2156   -2.8721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1406   -0.8079   -1.0934 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8815   -0.0532   -2.1906 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0290   -0.7196   -0.0260 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.7013    0.5780    0.2349 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1744    1.1192    1.3981 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2517    1.9081    2.0028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8334    3.0876    2.4384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2912    3.0825    2.0377 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0097    2.6229    3.1346 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7463    4.4646    1.6038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0545    4.9059    0.5013 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2707    2.1149    0.8838 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7752    2.7668   -0.2456 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0301   -2.8422   -0.5428 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3742   -4.0539   -1.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5246   -4.7165   -1.0263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9367   -5.8564   -1.7228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0991   -6.3281   -2.6956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5195   -7.4679   -3.3856 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0884   -5.7009   -2.9673 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4542   -4.5675   -2.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3415   -2.5332   -0.6172 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8752   -1.4965   -0.0437 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2107   -1.2074   -0.1464 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4471    0.7284    0.3181 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.3407    0.4973    1.3354 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8332    1.9180   -0.5676 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.0057    1.7032   -1.2372 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8499    3.1308    0.3543 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.7622    2.8846    1.3567 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4619    2.9297    2.7886 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7329    4.1924    2.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1673    2.4213    2.8374 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0337    4.2372    0.6399 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9578    1.0666    1.8924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4899    1.5856    1.6646 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2563    2.1583    2.5397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3282   -0.9770   -1.3125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6399   -2.9093   -0.7874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3132   -3.4975   -3.2496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0901   -1.7637   -3.5841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2238   -2.3010   -3.8307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1180   -0.5646   -0.6249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9345    0.2148   -2.2925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5164   -1.1562    0.8506 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7664    0.4545    2.0444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3785    3.9324    1.8384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6287    3.3003    3.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5441    1.8309    2.9190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8301    4.4437    1.5141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4728    5.1691    2.4438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0368    5.8826    0.4931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2139    1.5813    0.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7834    2.8385   -0.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2183   -4.3977   -0.2324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8952   -6.2995   -1.4483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0748   -7.2572   -4.2289 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7244   -6.0959   -3.7389 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3864   -4.0531   -2.4433 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8210   -1.8855   -0.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4744   -0.1615   -0.3725 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9781   -0.2471    1.1346 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9594    2.0170   -1.2815 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1586    2.4517   -1.8947 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1213    4.0459   -0.2125 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5844    2.5143    0.9149 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 17 20  1  0
 20 21  1  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  1
 27 29  1  0
 29 30  1  0
 27 31  1  0
 31 32  1  0
 13 33  2  0
 33 41  1  0
 41 42  1  0
 42 43  2  0
 33 34  1  0
 34 35  2  0
 35 36  1  0
 36 37  2  0
 37 38  1  0
 37 39  1  0
 39 40  2  0
  4 44  1  0
 44 45  1  0
 44 46  1  0
 46 47  1  0
 46 48  1  0
 48 49  1  0
 48  2  1  0
 43  6  1  0
 40 34  1  0
 42 10  1  0
 22 15  1  0
 31 24  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
  2 53  1  1
  4 54  1  1
  7 55  1  0
  9 56  1  0
 15 57  1  6
 17 58  1  1
 18 59  1  0
 18 60  1  0
 19 61  1  0
 20 62  1  1
 21 63  1  0
 22 64  1  1
 24 65  1  1
 26 66  1  0
 26 67  1  0
 28 68  1  0
 29 69  1  0
 29 70  1  0
 30 71  1  0
 31 72  1  6
 32 73  1  0
 43 79  1  0
 35 74  1  0
 36 75  1  0
 38 76  1  0
 39 77  1  0
 40 78  1  0
 44 80  1  6
 45 81  1  0
 46 82  1  6
 47 83  1  0
 48 84  1  6
 49 85  1  0
M  END


  Mrv1533004161523002D          

 49 54  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6194    1.3099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8743    2.0945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3894    2.7620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7250    3.5157    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6993    2.0945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1842    2.7620    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9543    1.3099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7389    1.0550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3520    1.6070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2657    2.4275    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0194    2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5715    2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1235    2.7631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2389    1.6650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1527    0.8446    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1590    1.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4945    0.6818    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
  6 17  1  0  0  0  0
 14 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  2  0  0  0  0
 18 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 28 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 26 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 38 42  1  0  0  0  0
 35 42  1  0  0  0  0
 42 43  1  0  0  0  0
  4 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
  2 48  1  0  0  0  0
 48 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0166367

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2=CC(O)=C3C(=O)C(OC4OC(CO)C(O)C4OC4OCC(O)(CO)C4O)=C(OC3=C2)C2=CC=C(O)C=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C31H36O18/c1-11-19(36)22(39)23(40)28(44-11)45-14-6-15(35)18-16(7-14)46-24(12-2-4-13(34)5-3-12)25(21(18)38)48-29-26(20(37)17(8-32)47-29)49-30-27(41)31(42,9-33)10-43-30/h2-7,11,17,19-20,22-23,26-30,32-37,39-42H,8-10H2,1H3

> <INCHI_KEY>
CZZJPZMXCROXOH-UHFFFAOYSA-N

> <FORMULA>
C31H36O18

> <MOLECULAR_WEIGHT>
696.611

> <EXACT_MASS>
696.190164319

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
67.12428342556059

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4H-chromen-4-one

> <ALOGPS_LOGP>
-0.27

> <JCHEM_LOGP>
-1.7085922189999987

> <ALOGPS_LOGS>
-2.37

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.556649243730341

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.083344341898591

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6122003587144

> <JCHEM_POLAR_SURFACE_AREA>
283.97999999999996

> <JCHEM_REFRACTIVITY>
158.60300000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.00e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      12.003  -5.390   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       6.756   2.445   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.232   3.910   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.327   5.156   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.953   6.563   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.772   3.910   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.677   5.156   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       9.248   2.445   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      10.713   1.969   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      11.857   3.000   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      11.696   4.531   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      13.103   5.158   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      14.133   4.013   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      15.164   5.158   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      15.379   3.108   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      15.218   1.577   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      13.363   2.680   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      13.990   1.273   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      -5.335  -0.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   48                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   44                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   16                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   25                                                  
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16    6                                                       
CONECT   18   14   19   24                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   18                                                       
CONECT   25   13   26                                                       
CONECT   26   25   27   33                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   26   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   42                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40   42                                             
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40                                                            
CONECT   42   38   35   43                                                  
CONECT   43   42                                                            
CONECT   44    4   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46    2   49                                                  
CONECT   49   48                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  108    0
END

View in JSmol

Synonyms

Value	Source
Kaempferol 3-apiosyl-(1->2)-a-L-arabinofuranoside-7-rhamnoside	Generator
Kaempferol 3-apiosyl-(1->2)-α-L-arabinofuranoside-7-rhamnoside	Generator

Chemical Formula

C₃₁H₃₆O₁₈

Average Mass

696.6110 Da

Monoisotopic Mass

696.19016 Da

IUPAC Name

3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]-4H-chromen-4-one

Traditional Name

3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one

CAS Registry Number

Not Available

SMILES

CC1OC(OC2=CC(O)=C3C(=O)C(OC4OC(CO)C(O)C4OC4OCC(O)(CO)C4O)=C(OC3=C2)C2=CC=C(O)C=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C31H36O18/c1-11-19(36)22(39)23(40)28(44-11)45-14-6-15(35)18-16(7-14)46-24(12-2-4-13(34)5-3-12)25(21(18)38)48-29-26(20(37)17(8-32)47-29)49-30-27(41)31(42,9-33)10-43-30/h2-7,11,17,19-20,22-23,26-30,32-37,39-42H,8-10H2,1H3

InChI Key

CZZJPZMXCROXOH-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cinnamomum burmanni	LOTUS Database	35616633
Cinnamomum osmophloeum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonoid-7-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavonoid glycosides

Direct Parent

Flavonoid-7-O-glycosides

Alternative Parents

Substituents

Flavonoid-7-o-glycoside
Flavonoid-3-o-glycoside
4'-hydroxyflavonoid
5-hydroxyflavonoid
Flavone
Hydroxyflavonoid
Phenolic glycoside
Chromone
Glycosyl compound
O-glycosyl compound
Benzopyran
1-benzopyran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Pyran
Monosaccharide
Benzenoid
Oxane
Monocyclic benzene moiety
Heteroaromatic compound
Vinylogous acid
Tertiary alcohol
Oxolane
Secondary alcohol
Acetal
Organoheterocyclic compound
Oxacycle
Polyol
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12111875 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-0.27	ALOGPS
logP	-1.7	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	7.08	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	283.98 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	158.6 m³·mol⁻¹	ChemAxon
Polarizability	67.12 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44258945

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one (NP0166367)

MOL for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

3D MOL for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

3D SDF for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

3D-SDF for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

PDB for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

3D PDB for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

SMILES for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

INCHI for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

Structure for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)

3D Structure for NP0166367 (3-[(3-{[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy}-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]chromen-4-one)